| Literature DB >> 10756425 |
M Mathieu1, M Helou, G Morin, P Dolhem, B Devauchelle, C Piussan.
Abstract
We report the sporadic case of a boy with clinical features of KBG syndrome, including slight mental retardation, characteristic facies, macrodontia, and skeletal anomalies.Entities:
Mesh：
Year: 2000 PMID： 10756425
Source DB: PubMed Journal: Genet Couns ISSN： 1015-8146